RecallHawk

Bethlehem Lights 10-inch Illuminated Ribbon Spheres

Bethlehem Lights LLC, of Naperville, Illinois

Summary

CPSC recall: Bethlehem Lights 10-inch Illuminated Ribbon Spheres. By Bethlehem Lights LLC, of Naperville, Illinois. Hazard: The LED lights on the recalled illuminated spheres can overheat, posing a risk of serious injury or death from a fire hazard.. Remedy: Consumers should stop using the recalled illuminated spheres immediately and contact Bethlehem Lights for a full refund. Consumers should immediately unplug the product from the wall and cut the power cord. To receive a refund, consumers wil

Details

Source

CPSC Consumer Product Recall

External ID

10786

Action Date

2026-05-21

Status

Recalled

Category

consumer_product

Product Description

The recalled Bethlehem Lights 10-inch Illuminated Ribbon Sphere is a spherical ornament made of reflective, silver-toned

Context & Analysis

This is a unclassified recall.

This was one of 21 consumer_product recalls issued in the same week, part of 47 consumer_product-related FDA actions this month.

Bethlehem Lights LLC, of Naperville, Illinois has 2 FDA actions in our database, including 1 recall.

Frequently Asked Questions

What is a FDA recall?

A Class III recall involves products that are unlikely to cause adverse health effects but violate FDA labeling or manufacturing regulations.

What should I do if I have this product?

Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Bethlehem Lights LLC, of Naperville, Illinois) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Bethlehem Lights LLC, of Naperville, Illinois have FDA actions?

Bethlehem Lights LLC, of Naperville, Illinois has 2 FDA actions in our database, including 1 recall and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "10786" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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